BESTMED: Observational Evaluation of Second Line Therapy Medications in Diabetes

NCT05161429 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 550000

Last updated 2023-06-22

No results posted yet for this study

Summary

An observational study of electronic patient data to compare diabetes medications and to determine which ones offer the best balance of risks and benefits.

Conditions

  • Diabetes Mellitus, Type 2

Interventions

DRUG

DPP4

Dipeptidyl peptidase-4 inhibitors (DPP4) including alogliptin, linagliptin, sitagliptin, and saxagliptin

DRUG

GLP-1 receptor agonist

Glucagon-like peptide-1 receptor agonists (GLP1-RA) including dulaglutide, exenatide, liraglutide and semaglutide

DRUG

Basal Insulin

degludec, detemir, glargine and NPH

DRUG

SLGT2

Sodium-glucose cotransporter-2 inhibitors (SLGT2) including canagliflozin, dapagliflozin, empagliflozin, and ertugliflozin

DRUG

SU

Sulfonylurea (SU) including glimepiride, glipizide, and glyburide

Sponsors & Collaborators

  • Patient-Centered Outcomes Research Institute

    collaborator OTHER
  • Baylor College of Medicine

    collaborator OTHER
  • Baylor Scott and White Research Institute

    collaborator UNKNOWN
  • The Cleveland Clinic

    collaborator OTHER
  • HealthCore, Inc.

    collaborator INDUSTRY
  • Humana Inc.

    collaborator INDUSTRY
  • Massachusetts General Hospital

    collaborator OTHER
  • Medical Outcomes Management

    collaborator UNKNOWN
  • University of Iowa

    collaborator OTHER
  • Allina Health

    collaborator UNKNOWN
  • Intermountain Health Care, Inc.

    collaborator OTHER
  • Marshfield Clinic

    collaborator UNKNOWN
  • Medical College of Wisconsin

    collaborator OTHER
  • University of Missouri-Columbia

    collaborator OTHER
  • University of Utah

    collaborator OTHER
  • Brigham and Women's Hospital

    lead OTHER

Principal Investigators

  • Alexander Turchin, MD, MS · Brigham and Women's Hospital

Eligibility

Min Age
30 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-07-01
Primary Completion
2024-06-30
Completion
2024-06-30
FDA Drug
Yes

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05161429 on ClinicalTrials.gov